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4H-pyran-4-one → N-[3-(Trifluoromethoxy)benzyl]tetrahydro-2H-pyran-4-amine

HRID 467952
ノート
印刷プレビュー

反応式

HRID 467952 の反応式
O=[C:2]1[CH:7]=[CH:6][O:5][CH:4]=[CH:3]1.[F:8][C:9]([F:20])([F:19])[O:10][C:11]1[CH:12]=[C:13]([CH:16]=[CH:17][CH:18]=1)[CH2:14][NH2:15].C(O[BH-](OC(=O)C)OC(=O)C)(=O)C.[Na+].[OH-].[Na+]>C(Cl)(Cl)Cl>[F:8][C:9]([F:19])([F:20])[O:10][C:11]1[CH:12]=[C:13]([CH:16]=[CH:17][CH:18]=1)[CH2:14][NH:15][CH:2]1[CH2:7][CH2:6][O:5][CH2:4][CH2:3]1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 79684H-pyran-4-oneHCID 14798Sodium HydroxideHCID 1452643-(Trifluoromethoxy)benzylamineHCID 5049666Sodium triacetoxyborohydride

生成物 1

HCID 58049381N-[3-(Trifluoromethoxy)benzyl]tetrahydro-2H-pyran-4-amine収率 82.2%

試薬・触媒・溶媒 1

HCID 6212
Chloroform
溶媒

実験手順

To a solution of 4-oxo-1H-pyran (200 mg) in chloroform (2 mL), 3-trifluoromethoxybenzylamine (380 mg) was added and the resulting mixture was stirred at room temperature for 30 minutes. Sodium (triacetoxy)borohydride (850 mg) was added and the resulting mixture was stirred for an hour. To the reaction mixture, an aqueous solution of 6 M sodium hydroxide was added and extraction was conducted with ethyl acetate. The solvents were distilled off under reduced pressure and the resulting residue was purified by column chromatography (NH silica gel cartridge; hexane/ethyl acetate=9:1 to 1:9) to give the titled compound (450 mg).

後処理

  1. stirringthe resulting mixture was stirred for an hour
  2. extractionextraction
  3. distillationThe solvents were distilled off under reduced pressure
  4. customthe resulting residue was purified by column chromatography (NH silica gel cartridge; hexane/ethyl acetate=9:1 to 1:9)

出典と根拠

ORDレコード
ord-8db1cfc7e3bc43d68e79f29d8b8cd4c2
出典データセット
uspto-grants-2014_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08623898B2

反応ノート

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